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Briefly, urine samples were centrifuged at 1,500 rpm for 10 min at room temperature, and the resulting cell pellets were washed twice with phosphate-buffered saline (PBS)

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Graphical Abstract Keywords Familial hypobetalipoproteinemia, Apolipoprotein B, Lipid metabolism disorder, Hepatic steatosis, Liver fibrosis, Monogenic liver disease Introduction Familial hypobetalipoproteinemia (FHBL) type 1 (OMIM 615558) is a rare, autosomal codominant monogenic disorder caused by variants in the apolipoprotein B ( APOB ) gene on chromosome locus 2p24.1

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10.1016/j.ejphar.2011.05.038 50 IlicS.DrmicD.ZarkovicK.KolencD.CoricM.BrcicL.et al (2010)

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